ArticleBMC research notes2008
Using a commercially available DNA extraction kit to obtain high quality human genomic DNA suitable for PCR and genotyping from 11-year-old saliva saturated cotton spit wads.
Article in BMC research notes, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
9 citing papers in PubMed, 15 citations in OpenAlex.
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- Paired design study by real-time PCR: miR-378* and miR-145 are potent early diagnostic biomarkers of human colorectal cancer.BMC cancer · 2015Article
- Candidate gene associations with withdrawn behavior.Journal of child psychology and psychiatry, and allied disciplines · 2013Article
- Article
- Identification and functional characterization of three novel alleles for the serotonin transporter-linked polymorphic region.Molecular psychiatry · 2012Article
- COMT Val158Met genotype as a risk factor for problem behaviors in youth.Journal of the American Academy of Child and Adolescent Psychiatry · 2010Article
- Human DNA extraction from whole saliva that was fresh or stored for 3, 6 or 12 months using five different protocols.Journal of applied oral science : revista FOBArticle
- Article
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundWe sought to describe the integrity of human genomic DNA extracted from saliva saturated cotton spit wads stored at -20 degrees C for approximately 11 years. 783 spit wad samples were collected from an ADHD sample population (Vermont Family Study) during 1996-2000. Human genomic DNA was extracted from the spit wads using a commercially available kit; QIAamp DNA Blood Midi Kit (Qiagen, Inc., Valencia, CA.) with a few modifications.
resultsThe resulting DNA yield was more than adequate for genetic analysis and ranged from approximately 1 mug to a total of 80 mug (mean 17.3 mugs +/- 11.9 mugs). A260/A280 ratios for the human genomic DNA extracted from the spit wads was consistently within the generally acceptable values of 1.7-2.0, with the lowest purity being 1.70, and a mean value of 1.937 +/- 0.226 for the 783 samples. The DNA also was suitable for PCR reactions as evidenced by the amplification of the serotonin-transporter-linked polymorphic region, 5HTTLPR. 5HTTLPR is a functional polymorphism in the promoter region of the serotonin transporter gene (HTT, SLC6A4, or SERT), consisting of two intensively studied alleles. 770 of the 783 samples (98.3%) produced fragments after PCR of the expected size with primers specific for 5HTTLPR.
conclusionHigh quality and abundant genomic DNA can be successfully retrieved from saliva saturated cotton spit wads using the commercially available kit, QIAamp DNA Blood Midi Kit from Qiagen, Inc. Furthermore, the DNA can be extracted in less than 3 hours and multiple samples can be processed simultaneously thus reducing processing time.
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.